Sp1 mediate hypoxia induced ephrinB2 expression via a hypoxia-inducible factor independent mechanism

被引:20
作者
Sohl, Marcus [1 ]
Lanner, Fredrik [1 ]
Farnebo, Filip [1 ,2 ]
机构
[1] Karolinska Inst, Dept Cell & Mol Biol, SE-17177 Stockholm, Sweden
[2] Karolinska Inst, Sect Plast Surg, Dept Mol Med & Surg, SE-17177 Stockholm, Sweden
关键词
Hypoxia; Arteriogenesis; EphrinB2; Promoter; Gene expression; Transcription factor; Sp1; CARDIOVASCULAR DEVELOPMENT; ENDOTHELIAL-CELLS; ARTERIAL IDENTITY; CIS-ELEMENTS; MAZ; DIFFERENTIATION; ANGIOGENESIS; RECEPTORS;
D O I
10.1016/j.bbrc.2009.10.146
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Environmental factors are instrumental in maintaining a healthy vasculature. Oxygen tension is higher in arteries than in veins and thus has the potential to be an Instructive signal in arterial/venous specification. EphrinB2 is specifically expressed in arteries and required during embryonic vessel formation. In this study, we show that expression of ephrinB2 is oxygen dependent Mutagenesis of hypoxia-responsive elements and transactivation experiments determined this regulation to be achieved in a hypoxia-inducible factor independent manner. MAZ and Sp1 are known to regulate transcription together and have been shown to bind to the same sites within prometers. Chromatin immunoprecipitation confirmed that binding of Sp1 to the ephrinB2 promoter was favored compared to MAZ under hypoxic relative to normoxic conditions Furthermore. siRNA mediated knockdown of Sp1 attenuated this hypoxic response These results indicate that hypoxia drives arterial differentiation by increasing ephrinB2 expression in endothelial cells through Sp1 activation (C) 2009 Elsevier Inc All rights reserved
引用
收藏
页码:24 / 27
页数:4
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